Canonical Allele Identifier: CA342748181

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155260389T>G (hg19) ; chr1:g.155290598T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155290598T>G , CM000663.2:g.155290598T>G	GRCh38
NC_000001.10:g.155260389T>G , CM000663.1:g.155260389T>G	GRCh37
NC_000001.9:g.153527013T>G	NCBI36
NG_011677.1:g.15837A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.1699A>C MANE Select	ENSP00000339933.4:p.Ile567Leu
ENST00000342741.4:c.1699A>C	ENSP00000339933.4:p.Ile567Leu
ENST00000392414.7:c.1606A>C	ENSP00000376214.3:p.Ile536Leu
NM_000298.5:c.1699A>C	NP_000289.1:p.Ile567Leu
NM_181871.3:c.1606A>C	NP_870986.1:p.Ile536Leu
XM_005245266.3:c.1858A>C	XP_005245323.1:p.Ile620Leu
XM_006711386.2:c.1507A>C	XP_006711449.1:p.Ile503Leu
XM_011509640.1:c.1507A>C	XP_011507942.1:p.Ile503Leu
NM_000298.6:c.1699A>C MANE Select	NP_000289.1:p.Ile567Leu
XM_006711386.4:c.1507A>C	XP_006711449.1:p.Ile503Leu
XM_011509640.3:c.1507A>C	XP_011507942.1:p.Ile503Leu
NM_181871.4:c.1606A>C	NP_870986.1:p.Ile536Leu